The basic helix-loop-helix leucine zipper transcription factor Mitf is conserved in Drosophila and functions in eye development

被引:64
作者
Hallsson, JH
Haflidadóttir, BS
Stivers, C
Odenwald, W
Arnheiter, H
Pignoni, F
Steingrímsson, E
机构
[1] Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA 02114 USA
[2] Univ Iceland, Fac Med, IS-101 Reykjavik, Iceland
[3] NINDS, Lab Dev Neurogenet, NIH, Bethesda, MD 20892 USA
[4] Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA
[5] NINDS, Neural Cell Fate Determinants Sect, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1534/genetics.167.1.233
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The MITF protein is a member of the MYC family of basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factors and is most closely related to the TFE3, TFEC, and TFEB proteins. In the mouse, MITF is required for the development of several different cell types, including the retinal pigment epithelial (RPE) cells of the eye. In Mitf mutant mice, the presumptive RPE cells hyperproliferate, abnormally express the retinal transcriptional regulator Pax6, and form an ectopic neural retina. Here we report the structure of the Mitf gene in Drosophila and demonstrate expression during embryonic development and in the eye-antennal imaginal disc. In vitro, transcriptional regulation by Drosophila Mitf, like its mouse counterpart, is modified by the Eyeless (Drosophila Pax6) transcription factor. In vivo, targeted expression of wild-type or dominant-negative Drosophila Mitf results in developmental abnormalities reminiscent of Mitf function in mouse eye development. Our results suggest that the Mitf gene is the original member of the Mitf-Tfe subfamily of bHLH-Zip proteins and that its developmental function is at least partially conserved between vertebrates and invertebrates. These findings further support the common origin of the vertebrate and invertebrate eyes.
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页码:233 / 241
页数:9
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